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나노물질및화학반응연구단
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Ultrafast charge transfer coupled with lattice phonons in two-dimensional covalent organic frameworks

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dc.contributor.authorTae Wu Kim-
dc.contributor.authorSunhong Jun-
dc.contributor.authorYoonhoo Ha-
dc.contributor.authorRajesh K. Yadav-
dc.contributor.authorAbhishek Kumar-
dc.contributor.authorChung-Yul Yoo-
dc.contributor.authorInhwan Oh-
dc.contributor.authorHyung-Kyu Lim-
dc.contributor.authorJae Won Shin-
dc.contributor.authorRyong Ryoo-
dc.contributor.authorHyungjun Kim-
dc.contributor.authorJeongho Kim-
dc.contributor.authorJin-Ook Baeg-
dc.contributor.authorHyotcherl Ihee-
dc.date.available2019-10-11T08:10:32Z-
dc.date.created2019-05-29-
dc.date.issued2019-04-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/6313-
dc.description.abstract© 2019, The Author(s). Covalent organic frameworks (COFs) have emerged as a promising light-harvesting module for artificial photosynthesis and photovoltaics. For efficient generation of free charge carriers, the donor–acceptor (D-A) conjugation has been adopted for two-dimensional (2D) COFs recently. In the 2D D-A COFs, photoexcitation would generate a polaron pair, which is a precursor to free charge carriers and has lower binding energy than an exciton. Although the character of the primary excitation species is a key factor in determining optoelectronic properties of a material, excited-state dynamics leading to the creation of a polaron pair have not been investigated yet. Here, we investigate the dynamics of photogenerated charge carriers in 2D D-A COFs by combining femtosecond optical spectroscopy and non-adiabatic molecular dynamics simulation. From this investigation, we elucidate that the polaron pair is formed through ultrafast intra-layer hole transfer coupled with coherent vibrations of the 2D lattice, suggesting a mechanism of phonon-assisted charge transfer-
dc.description.uri1-
dc.language영어-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleUltrafast charge transfer coupled with lattice phonons in two-dimensional covalent organic frameworks-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000465201500006-
dc.identifier.scopusid2-s2.0-85064922747-
dc.identifier.rimsid68130-
dc.contributor.affiliatedAuthorTae Wu Kim-
dc.contributor.affiliatedAuthorInhwan Oh-
dc.contributor.affiliatedAuthorJae Won Shin-
dc.contributor.affiliatedAuthorRyong Ryoo-
dc.contributor.affiliatedAuthorHyotcherl Ihee-
dc.identifier.doi10.1038/s41467-019-09872-w-
dc.identifier.bibliographicCitationNATURE COMMUNICATIONS, v.10, no.1, pp.1873-
dc.citation.titleNATURE COMMUNICATIONS-
dc.citation.volume10-
dc.citation.number1-
dc.citation.startPage1873-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusELECTRON-HOLE RECOMBINATION-
dc.subject.keywordPlusTOTAL-ENERGY CALCULATIONS-
dc.subject.keywordPlusVIBRATIONAL COHERENCE-
dc.subject.keywordPlusPYXAID PROGRAM-
dc.subject.keywordPlusDYNAMICS-
dc.subject.keywordPlusFEMTOSECOND-
dc.subject.keywordPlusSTATES-
dc.subject.keywordPlusBAND-
dc.subject.keywordPlusSPECTROSCOPY-
dc.subject.keywordPlusEXCITATION-
Appears in Collections:
Center for Nanomaterials and Chemical Reactions(나노물질 및 화학반응 연구단) > 1. Journal Papers (저널논문)
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